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Completed Phase 1 Interventional

A Study of ART24 in Subjects Recently Cured of a Clostridioides Difficile Infection (CDI)

ClinicalTrials.gov ID: NCT04891965

Public ClinicalTrials.gov record NCT04891965. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:21 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Placebo-Controlled, Double-Blind, Phase 1 Study of ART24 in Subjects Recently Cured of a Clostridioides Difficile Infection (CDI)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a randomized, placebo-controlled, double-blind, multi-site study in which up to approximately 36 subjects with a recent C. difficile infection (CDI) who have completed a standard of care course of CDI antibiotics and have achieved clinical cure based on signs and symptoms, will be randomized to 7 or 28 daily doses of ART24 or placebo. Subjects will be followed for 6 months after the last dose of study drug.

Study identification

NCT ID
NCT04891965
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Adiso Therapeutics
Industry
Enrollment
36 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 27, 2020 (Actual)
Primary completion
Jul 7, 2022 (Actual)
Completion
Oct 13, 2022 (Actual)
Last update posted
Oct 17, 2022

2020 – 2022

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Palmtree Clinical Research Palm Springs California 92262 —
Gastro Florida Clearwater Florida 33765 —
Doral Medical Research Doral Florida 33166 —
Louisiana Research Center Shreveport Louisiana 71105 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
Mayo Clinic Rochester Minnesota 55905 —
Mercury Street Medical Group Butte Montana 59701 —
DiGiovanna Institute Massapequa New York 11758 —
NYU Grossman School of Medicine New York New York 10016 —
Weill Cornell Medicine New York New York 10021 —
Montefiore Medical Center The Bronx New York 10467 —
Frontier Clinical Research, LLC Uniontown Pennsylvania 15401 —
Advanced Clinical Research Riverton Utah 84065 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04891965, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 17, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04891965 live on ClinicalTrials.gov.

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